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189 AGXT

189

AGXT

alanine--glyoxylate and serine--pyruvate aminotransferase

protein-coding

Homo sapiens

基因描述

Type Description
Definition alanine--glyoxylate and serine--pyruvate aminotransferase

研究结论

Date Results Publications
2020-09-19 16:27:00 Loss of alanine-glyoxylate and serine-pyruvate aminotransferase expression accelerated the progression of hepatocellular carcinoma and predicted poor prognosis. 31771612
2020-07-25 10:54:00 two human constructs, wild-type and engineered AGT (RHEAM), were tested in Agxt(-/-) mice. Repeat dosing in Agxt(-/-) mice resulted in a 40% reduction in urinary oxalate, suggesting therapeutic benefit. 30676254
2020-07-11 12:37:00 novel mutation c. 799A>T p. (IIe267Phe) detected in primary hyperoxaluria type 1 patient and family 32569165
2020-01-11 12:40:00 Expression of the primary hyperoxaluria type 1-causal gene AGXT can be regulated at the posttranscriptional level by miR-4660. 30852714
2019-10-26 10:12:00 The most common AGXT gene mutation found in Libyan children with primary hyperoxaluria type 1 was c.731T>C (p.lle244thr) and this is more likely due to the strong genetic pooling caused by the high consanguinity rate. 29456205

名称对应

Type IDs
Synonymous AGT, AGT1, AGXT1, PH1, SPAT, SPT, TLH6
Gene
UniProtKB-ID: SPYA_HUMAN
UniprotKB: P21549
UniParc: UPI0000135E9B
EMBL: CH471063, AC104809, X53414, D13368, BC132819, M61763, X56092, AK292754
Ensembl: ENSG00000172482
KO: hsa:189
Nucleutide sequences
EMBL-CDS: AAA51680.1, CAA39572.1, CAA37493.1, BAA02632.1, BAF85443.1, EAW71222.1, AAY24168.1, AAI32820.1
Ensembl_TRS: ENST00000307503
Protein sequencees
Ensembl_PRO: ENSP00000302620
RefSeq: NP_000021.1
Others
UniRef100: UniRef100_P21549
UniRef90: UniRef90_P21549
UniRef50: UniRef50_P21549
UniGene: Hs.144567
CCDS: CCDS2543.1

全选

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